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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632284Generated: November 2, 2026

N-Benzoylcytidine → HCID 178418385, compound

https://huagongshe.com/reaction/1632284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BenzoylcytidineHCID 10066259—
ReactantHCID 178420932HCID 178420932—
ReactantHCID 178527074HCID 178527074—
SolventAcetonitrileHCID 6342—
ProductHCID 178418385HCID 178418385—
ProductHCID 178418441HCID 178418441—

Reaction Steps

N-Benzoylcytidine linked from the 3' hydroxyl group via a hemisuccinate bridge to aminopropyl-substituted HPLC-grade silica (Vydac) was used as the solid-phase support. Samples (100 mg each; 10 micromoles) were shaken in sealed test tubes in acetonitrile (1 ml) with each of the four 5'-dimethoxytrityl-deoxynucleoside-3'-dimethylaminophosphoramidites and either tetrazole (1 mmole) or benzotriazole (600 micromoles) to form the tetrazolide or benzotriazolide-phosphite active species, the latter being a compound of this invention. After thorough washing by repeated centrifugation and subsequent decanting, and oxidation with 0.01M iodine, the support was treated with 2.75% (w/v) trichloroacetic acid in methylene chloride (10 ml) for 5 minutes. Spectrophotometric assay of the dimethoxytrityl carbonium ion produced in the supernatant demonstrated that all couplings had proceeded to greater than 95% of theoretical yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474948
Source datasetuspto-grants-1984_10
ORD IDord-a7da0d4ca9bf4f2bab299c45fcc0c396
Source noteuspto-grants-1984_10